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Chemical Structure| 61070-98-2 Chemical Structure| 61070-98-2

Structure of 61070-98-2

Chemical Structure| 61070-98-2

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Product Details of [ 61070-98-2 ]

CAS No. :61070-98-2
Formula : C4H6N4
M.W : 110.12
SMILES Code : NC1=NN=CC=C1N
MDL No. :MFCD01646101
Boiling Point : No data available
InChI Key :BXFLYXZXQZSHOZ-UHFFFAOYSA-N
Pubchem ID :6405709

Safety of [ 61070-98-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of [ 61070-98-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 61070-98-2 ]

[ 61070-98-2 ] Synthesis Path-Downstream   1~8

  • 2
  • [ 61070-98-2 ]
  • [ 695-91-0 ]
  • 3
  • CH3 I [ No CAS ]
  • S-methyl-2-methoxy-4-propargyloxythiobenzoic acid morpholide iodide [ No CAS ]
  • [ 61070-98-2 ]
  • 2-methoxy-4-(prop-2-yn-1-yloxy)benzaldehyde [ No CAS ]
  • 2-(2-methoxy-4-propargyloxyphenyl)-1,3,5,6-tetraazaindene [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogen sulfide; In morpholine; ethylene glycol; acetone; EXAMPLE 6 A mixture of 4.33 g of S-methyl-2-methoxy-4-propargyloxythiobenzoic acid morpholide iodide (obtainable by boiling 2-methoxy-4-propargyloxybenzaldehyde with sulfur in morpholine and then reacting with CH3 I in acetone), 1.1 g of IIb and 35 ml of ethylene glycol is heated at 130 for 40 minutes, and poured into ice-water, which is filtered to give 2-(2-methoxy-4-propargyloxyphenyl)-1,3,5,6-tetraazaindene, m.p. 224.
  • 4
  • [ 88710-28-5 ]
  • [ 61070-98-2 ]
  • 2-(4-cyanomethoxy-2-methoxyphenyl)-1,3,5,6-tetraazaindene hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
With trichlorophosphate; EXAMPLE 8 2.78 g of 2-methoxy-4-cyanomethoxybenzoic acid morpholide are mixed with 1.1 g of IIb, 5 ml of POCl3 are added dropwise with stirring, and the mixture is boiled for 3 hours and evaporated to dryness. The customary working up gives 2-(4-cyanomethoxy-2-methoxyphenyl)-1,3,5,6-tetraazaindene, hydrochloride, m.p. 268.
  • 5
  • [ 2150-41-6 ]
  • [ 61070-98-2 ]
  • 2-(2,4-dimethoxyphenyl)-1,3,5,6-tetraazaindene [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; trichlorophosphate; EXAMPLE 4 A mixture of 11 g of IIb, 19.6 g of methyl 2,4-dimethoxybenzoate and 300 ml of POCl3 is heated at 120 for 2 hours, and evaporated to dryness, and the residue is treated with 2N hydrochloric acid. This gives 2-(2,4-dimethoxyphenyl)-1,3,5,6-tetraazaindene, m.p. 268.
  • 6
  • 2-methoxy-4-propargyloxy-benzoic acid [ No CAS ]
  • [ 61070-98-2 ]
  • 3-amino-4-(2-methoxy-4-propargyloxybenzoylamino)-pyridazine [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine; thionyl chloride; triethylamine; In water; benzene; EXAMPLE 3 2.06 g of 2-methoxy-4-propargyloxybenzoic acid are boiled together with 7 ml of benzene and 4 ml of SOCl2 for 1 hour, the mixture is evaporated to dryness, and the residue is dissolved in 5 ml of benzene. The solution of the acid chloride is added dropwise to a mixture of 1.1 g of IIb, 7 ml of pyridine and 5 ml of triethylamine. The resulting mixture is stirred at 20 for 2 hours, water is added, and the resulting mixture is neutralised with hydrochloric acid and worked up as customary. The 3-amino-4-(2-methoxy-4-propargyloxybenzoylamino)-pyridazine obtained is converted into the corresponding hydrochloride, and the latter (200 mg) is dissolved in 2 ml of pyridine.
  • 7
  • [ 88710-29-6 ]
  • [ 61070-98-2 ]
  • 2-(4-cyanomethoxy-2-methoxyphenyl)-1,3,5,6-tetraazaindene hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium bissulfite; In ISOPROPYLAMIDE; EXAMPLE 11 11 g of IIb and 18.9 g of 2-methoxy-4-cyanomethoxybenzaldehyde are dissolved in 100 ml of dimethylacetamide, on addition of 19 g of sodium disulfite the solution is stirred at 140 for two hours and then worked up as customary to give 2-(4-cyanomethoxy-2-methoxyphenyl)-1,3,5,6-tetraazaindene, hydrochloride, m.p. 268.
  • 8
  • [ 4519-39-5 ]
  • [ 61070-98-2 ]
  • [ 1105062-83-6 ]
YieldReaction ConditionsOperation in experiment
2,3-Difluoro-benzoic acid (lOOmg), HATU (345.6 mg), and diisopropylethylamine (3 eq.) were added to DMF (90OuL) and stirred for 15 minutes. Pyridazine-3,4-diamine was added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was evaporated, partitioned between water and ethyl acetate. The organic fraction was dried with sodium sulfate and concentrated in vacuo. The residue was then heated in acetic acid at reflux for one day. The mixture was evaporated and purified via reverse-phase HPLC to give 136 mg of 6-(2,3-difluoro-phenyl)-2H- imidazo[4,5-c]pyridazine. MS: 233.1 (M+H+) H'-NMR (DMSOd6): £(prhom) 9.04 (d, IH, 5.8Hz), 8.08 (m, IH), 7.96 (d, IH, 5.3 Hz) 7.70 (m, IH) 7.44 (m, IH)
General Procedure JSynthesis of Compounds 245-2476-(2,3-difluoro-phenyl)-2H-imidazo[4,5-c]pyridazinePyridazine-3,4-diamine was synthesized as described by Kuraishi et al. in J. Het. Chem. 1964, 1, 42-47. MS: 111.1 (M+H+); H1-NMR (DMSO-d6): delta (ppm) 8.2-8.3 (m, 3H), 7.31 (s, 2H), 6.73 (d, 1H, 6.1 Hz).2,3-Difluoro-benzoic acid (100 mg), HATU (345.6 mg), and diisopropylethylamine (3 eq.) were added to DMF (900 uL) and stirred for 15 minutes. Pyridazine-3,4-diamine was added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was evaporated, partitioned between water and ethyl acetate. The organic fraction was dried with sodium sulfate and concentrated in vacuo. The residue was then heated in acetic acid at reflux for one day. The mixture was evaporated and purified via reverse-phase HPLC to give 136 mg of 6-(2,3-difluoro-phenyl)-2H-imidazo[4,5-c]pyridazine. MS: 233.1 (M+H+) H1-NMR (DMSO-d6): delta (ppm) 9.04 (d, 1H, 5.8 Hz), 8.08 (m, 1H), 7.96 (d, 1H, 5.3 Hz) 7.70 (m, 1H) 7.44 (m, 1H)
 

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